Taiwan FDA registration 57246ecc40fd3f4b8d6e1464e6baa43b

Ke Lang Clear silicone water gel progressive multifocal daily throw contact lenses

TW: 珂朗清矽水膠漸進多焦點每日拋隱形眼鏡
Taiwan flagTaiwan·Risk Class 2·COOPERVISION MANUFACTURING LTD.;; COOPERVISION CL KFT;; 頂典有限公司·Registered Apr 19, 2016 – Apr 19, 2026Expired
Registration details
Analysis ID
57246ecc40fd3f4b8d6e1464e6baa43b
Customs Code
DHA05602851400
Company information
Manufacturer Country
Taiwan, Province of China;;United Kingdom;;Hungary
Authorized Representative
COOPERVISION (TAIWAN) CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5925 軟式隱形眼鏡
Import Information
import
Dates and status
Registration Date
Apr 19, 2016
Expiry Date
Apr 19, 2026
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About this record

Access comprehensive regulatory information for Ke Lang Clear silicone water gel progressive multifocal daily throw contact lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57246ecc40fd3f4b8d6e1464e6baa43b and manufactured by COOPERVISION MANUFACTURING LTD.;; COOPERVISION CL KFT;; 頂典有限公司. The authorized representative in Taiwan is COOPERVISION (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including COOPERVISION MANUFACTURING LTD., CooperVision Manufacturing Costa Rica, SRL; COOPERVISION, INC., and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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